ClinVar Miner

List of variants in gene MYH14 reported as benign for Nonsyndromic Hearing Loss, Dominant

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Total variants: 8
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HGVS dbSNP
NM_001145809.2(MYH14):c.*216T>G rs627491
NM_001145809.2(MYH14):c.2250A>G (p.Pro750=) rs1651553
NM_001145809.2(MYH14):c.2355-14C>T rs12981413
NM_001145809.2(MYH14):c.3018G>A (p.Leu1006=) rs3745504
NM_001145809.2(MYH14):c.3033+11T>C rs930086
NM_001145809.2(MYH14):c.5430G>A (p.Ser1810=) rs3745509
NM_001145809.2(MYH14):c.5678+12C>T rs3826772
NM_001145809.2(MYH14):c.657G>A (p.Ala219=) rs4801822

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